RIVA, PAOLA VANDA

RIVA, PAOLA VANDA  

Dipartimento di Biotecnologie Mediche e Medicina Traslazionale  

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Titolo Data di pubblicazione Autori Tipo File Abstract
19p deletion in recurring leiomyosarcoma lesions from the same patient 2000 P. RivaV. GualandriM. VolontèM. MiozzoA. F. ContiL. Larizza + Article (author) -
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas 2006 M. StroppiP. Riva + Article (author) -
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism 1995 P. RivaL. Larizza + Article (author) -
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene 1996 P. RivaL. Larizza Article (author) -
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome 2010 E. MartinoliG.V. ZuccottiM. VolontèM. VenturinP.V. Riva + Article (author) -
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort 2023 Paola BettinaglioEleonora ManganoViviana TrittoClaudia CesarettiRoberta BordoniMarco MoscatelliPaola Riva + Article (author) -
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36 2000 M. MiozzoP. RivaM. VolontèF. MacciardiL. LarizzaA. M. Fuhrman Conti + Article (author) -
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome 2014 M. VenturinS. CarraG. GaudenziG.R. GalloS. MonciniF. CotelliP. Riva + Article (author) -
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele 2008 F. OrzanM. StroppiM. VenturinP. Riva + Article (author) -
Centa2 is expressed during heart development and is a candidate gene for CVMs 2008 M. VenturinG. GaudenziM. StroppiM. CrippaF. CotelliP. Riva + Conference Object -
Centa2 è espresso durante lo sviluppo del cuore ed è un gene candidato per le malformazioni cardiovascolari 2008 M. VenturinM. StroppiG. GaudenziF. CotelliP. Riva + Conference Object -
Centaurin-α2 and tubulin interaction increases microtubule stability 2010 M. StroppiD. CartelliG. CappellettiM. VenturinE. BattaglioliP. Riva + Article (author) -
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules 2012 P. ZuccottiD. CartelliV. PandiniM. VenturinA. AlivertiE. BattaglioliG. CappellettiP.V. Riva + Article (author) -
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes 2023 Tritto, VivianaCapitanio, DanieleGelfi, CeciliaRiva, Paola Article (author) -
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes 2022 Tritto, VivianaRusconi, FrancescoRiva, Paola + Article (author) -
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome 1996 P. RivaL. DonedaL. Larizza + Article (author) -
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements 2006 M. VenturinA. PatriziMARTINOLI, EMANUELAP. Riva + Article (author) -
Characterization of breakpoint boundaries in 19 Neurofibromatosis type 1 microdeletions 2005 C. GervasiniM.VenturinP.RivaL. Larizza + Article (author) -
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms 2008 P. RivaLONGONI, MAURO Book Part (author) -
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome 1998 M. MiozzoP. RivaA. M. Fuhrman ContiL. VolpiL. Larizza + Article (author) -